Clinical Research Coordinator II - Remote

Overview

The Clinical Research Coordinator II will work independently to enroll patients in clinical research protocols and manage data collection for cancer studies, ensuring compliance with regulations.

In Short

• Enrolling patients for clinical research studies.
• Managing data collection and submission.
• Acting as a liaison between clinical teams and sponsors.
• Ensuring compliance with institutional and federal regulations.
• Assisting in Quality Control and Training & Development.
• Conducting data entry and quality checks.
• Preparing for audits and monitoring visits.
• Drafting and submitting IRB applications.
• Supporting project management activities.
• Maintaining communication with research teams.

Requirements

• Bachelor's Degree in a related field.
• Experience in clinical research or compliance required.
• Strong organizational and time management skills.
• Excellent written and verbal communication skills.
• Ability to work independently and as part of a team.
• Knowledge of clinical research trends.
• Ability to mentor others.
• Problem identification and solution development skills.

Benefits

• Opportunity to work on innovative research projects.
• Involvement in patient-centered care initiatives.
• Collaboration with a dynamic team of professionals.
• Professional development opportunities.
• Supportive work environment.